5 - HT1B受体拮抗剂异莫烷对西酞普兰预处理雄性大鼠射精行为的刺激作用

S. Ahlénius, K. Larsson
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引用次数: 3

摘要

先前的研究表明,阻断5-HT1A受体揭示了选择性5-羟色胺(5-HT)再摄取抑制剂西酞普兰对雄性大鼠射精行为的抑制作用。本文报道了选择性5-羟色胺再摄取抑制剂西酞普兰(10 mgkg - 1)皮下(s.c c)促进了5-羟色胺受体拮抗剂异莫坦(4 mgkg - 1, s.c c)治疗的雄性Wistar大鼠的射精行为,而单独西酞普兰和异莫坦都没有任何影响。结论是西酞普兰对雄性大鼠射精行为具有抑制作用,这种抑制作用通常由5-HT1A受体介导的促进作用平衡。
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Stimulation of Ejaculatory Behaviour by the 5‐HT1B Receptor Antagonist Isamoltane in Citalopram‐pretreated Male Rats
It has previously been shown that blocking 5-HT1A receptors unmasks an inhibitory action of the selective 5-hydroxytryptamine (5-HT) re-uptake inhibitor citalopram on male rat ejaculatory behaviour. This paper reports that subcutaneous (s.c.) administration of the selective 5-HT re-uptake inhibitor citalopram (10 mgkg−1) facilitated ejaculatory behaviour in male Wistar rats treated with the 5-HT1B receptor antagonist isamoltane (4 mgkg−1, s.c.), whereas neither citalopram nor isamoltane alone had any effect. It is concluded that citalopram possesses an inhibitory action on male rat ejaculatory behaviour, and that this inhibition normally is balanced by a facilitatory action mediated via 5-HT1A receptors.
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